Emily Bonkowski

1.2k citations
11 papers · 296 · h-index 4

Impact in

Papers in

    • Genomics and Rare Diseases 5
    • Genetics and Neurodevelopmental Disorders 4
    • BRCA gene mutations in cancer 3
    • Neurogenetic and Muscular Disorders Research 1
    • DNA Repair Mechanisms 2

Emily Bonkowski

11 papers receiving 296 citations

Peers

Emily Bonkowski
Comparison fields: 5 of 47
  • Hematology 74
  • Physiology 13
  • Genetics 27
  • Genetics 70
  • Immunology 50
Replace Mefford Hc with:
Mefford Hc
Fong Ct United States
Xiaodan Ding China
Leïla Lazaro France
Linda Manwaring United States
Katerina Vlahos Australia
Isabelle Millard Belgium
C R Müller Germany
SJ Greenberg United States
Aiyin Liao United Kingdom
Emily Bonkowski relative to Mefford Hc Mefford Hc's profile →
Citations per field
00.5×10×20×29×
Mefford Hc · 1×
Citations per year

Countries citing papers authored by Emily Bonkowski

Since Specialization
Citations

This map shows the geographic impact of Emily Bonkowski's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Emily Bonkowski with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emily Bonkowski more than expected).

Fields of papers citing papers by Emily Bonkowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emily Bonkowski. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Emily Bonkowski. The network helps show where Emily Bonkowski may publish in the future.

Co-authors

The 25 scholars most cited alongside Emily Bonkowski, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Emily Bonkowski Line = papers co-authored together Emily Bonkowski links everyone, so they are left out of the graph.

All Works

11 of 11 papers shown
#Work
1 2016127
2 2013106
3 201342
4 20228
5 20233
6 20252
7 20242
8 20242
9 20152
10 20241
11 20231

About Emily Bonkowski

Emily Bonkowski is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 11 papers that have together received 296 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), BRCA gene mutations in cancer (3 papers), DNA Repair Mechanisms (2 papers), Autism Spectrum Disorder Research (1 paper), Cancer Genomics and Diagnostics (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Endoplasmic Reticulum Stress and Disease (1 paper). The work is most often cited by research in Hematology (74 citations), Physiology (13 citations), Genetics (27 citations), Genetics (70 citations) and Immunology (50 citations). Emily Bonkowski has collaborated with scholars based in United States, Germany and Japan. Frequent co-authors include Wendy H. Raskind, Thomas D. Bird, Deborah A. Nickerson, Youngmee Sul, John Wolff, Mark Matsushita, Dong-Hui Chen, Jennifer E. Below, Akiko Shimamura and Toshiyasu Taniguchi. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, Public Health Genomics, The American Journal of Human Genetics and JCO Precision Oncology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact